A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697011



Internal ID15433663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25873913..25881990hg38UCSC Ensembl
Innerchr15:26119060..26127137hg19UCSC Ensembl
Innerchr15:23670153..23678230hg18UCSC Ensembl
Innerchr15:23670153..23678230hg17UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg388078
hg198078
hg188078
hg178078
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519720
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697011
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer